List of variants in gene MLH3 reported as likely benign by Mayo Clinic Laboratories, Mayo Clinic

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 11

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HGVS	dbSNP	gnomAD frequency
NM_001040108.2(MLH3):c.666G>A (p.Lys222=)	rs28756980	0.01977
NM_001040108.2(MLH3):c.444G>C (p.Val148=)	rs11556091	0.01944
NM_001040108.2(MLH3):c.4242+13C>G	rs77157930	0.01890
NM_001040108.2(MLH3):c.3570+28A>T	rs67547819	0.00949
NM_001040108.2(MLH3):c.408T>C (p.Asp136=)	rs61755655	0.00552
NM_001040108.2(MLH3):c.3987+15C>T	rs117251698	0.00496
NM_001040108.2(MLH3):c.4242+28G>C	rs188956387	0.00128
NM_001040108.2(MLH3):c.3571-26G>T	rs369710216	0.00069
NM_001040108.2(MLH3):c.3828-15A>C	rs200169541	0.00005
NM_001040108.2(MLH3):c.3716-10C>T	rs374204567	0.00001
NM_001040108.2(MLH3):c.3828-24del	rs761256304

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